Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2445-2024 — LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00

U.S. FDA — Device Enforcement · United States · 2024-06-27 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2445-2024
Date of alert
2024-06-27
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
LINK BIO CORP
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04026575310203
Reported risk: The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down into the laser marking process.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.